Video & movements recording: Video recording of face, body movements and physiological parameters (heart rate, conductance using a wireless watch) of the participants during the blood test
Questionnaires: Passing self and hetero questionnaires of emotion felt and perceived.
Study summary
The project is a prospective study designed to characterize behaviour and its psycho-physiological correlates of participants with ASD (children and adults) in comparison with subjects without ASD matched in age during blood test in common practice.
Eligibility
Sex
ALL
Min age
6 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria:
All participants :
* Person over 6 years of age
* Person who consent to participate in the study
* Membership of the social security scheme
* Person who not received analgesic treatment that may interfere with pain perception
* Person with medical prescription for blood sample
Participants with ASD :
* Person with ASD diagnosis
* If applicable, legal authority consent to participate in the study
Exclusion Criteria:
All participants :
* Person with unstabilized drug therapy
* Person with acute or chronic pain
* Person with pathology or receiving a treatment which can have an impact in modification of the pain
* Person with oculomotor and/or neuro-motor disorders
* Pregnant or breastfeeding woman
* Person with deprivation of liberty
* Person who no consent to participate in the study or no consent to realised video recording
Participants without ASD :
* Protected adult
* Person with ASD diagnosis
Primary outcome measure(s)
Facial expression during blood sample — through study completion, an average of 1 to 6 months Evaluation of facial expression during blood sample in people with ASD as compared to healthy people with Face reader, Noldus sofware.
Body movement during blood sample — through study completion, an average of 1 to 6 months Evaluation of body movement during blood sample in people with ASD as compared to healthy people with EMPATICA watch and Face, Legs, Activity, Cry, Consolabilty (FLACC) scale
Trial sites (1)
Facility
City
Region
Status
Centre Hospitalier Charles PERRENS
Bordeaux
France
Recruiting
More Centre Hospitalier Charles Perrens, Bordeaux trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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